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NCT Number: NCT06198907

Golidocitinib in Combination With Sintilimab for PD-L1 Selected Treatment Locally Advanced or Metastatic Non-Small Cell Lung Cancer(NSCLC)

This is a phase 2 Study to investigate the safety, tolerability, and anti-tumor activity of golidocitinib in combination with sintilimab as the front-line treatment for patients with metastatic PD-L1 positive non-small cell lung cancer (NSCLC)

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Cancer Institute and Hospital, Chinese Academy of Medical Sciences

Beijing, Beijing Municipality, 100021, China

Location contact

Jie Wang, MD, PhD

CONTACT

[email protected]

010-87788219

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Be able to provide a signed and dated, written informed consent.
  • Adults aged ≥18 to 75 years.
  • ECOG performance status 0-1.
  • Predicted life expectancy ≥ 12 weeks
  • Histologically or cytologically confirmed non-small-cell lung cancer (NSCLC) , Stage IIIB/IIIC (not suitable for concomitant chemoradiotherapy) or Stage IV according to AJCC 8th
  • Without EGFR or ALK mutations.
  • Adequate bone marrow reserve and organ system functions.
  • Patients with stable and symptomatic brain metastasis (BM) can be enrolled.

Part A Dose escalation:

Patients must have relapsed after or been refractory/intolerant to ≥ 1 prior systemic therapy(ies) for NSCLC

Part B dose expansion:

  • At least one measurable lesion according to RECIST 1.1.
  • Previously systemic untreated for advanced disease.
  • PD-L1 TPS ≥ 50% (cohort 1), PD-L1 TPS 1-49% (cohort 2)

Exclusion criteria

  • Histopathology confirmed a mixture of NSCLC and small-cell lung cancer
  • Known active central nervous system (CNS) metastases and/or carcinomatous meningitis.
  • Prior malignancy within 5 years
  • History of organ transplantation or hematopoietic stem cell transplantation
  • Sever lung function decline or interstitial lung disease that has required oral or IV steroids
  • Active autoimmune disease requiring systemic therapy within 2 years
  • Immunodeficiency, or being treated with immunosuppressive therapy (including systemic glucocorticoid) within 7 days prior to the first dose of study treatment.
  • Active infections
  • Significant cardiac disorder
  • Other serious or uncontrolled systemic diseases assessed by the investigator.

Part A Dose escalation:

  • Prior systemic therapy with an anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137, or stimulatory or synergistic T-cell receptor (CTLA-4、OX-40、CD137) within 4 weeks

Part B Dose Expansion:

  • Any prior systemic anti-tumor therapy
  • Prior systemic immunotherapy, including anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137, or stimulatory or synergistic T-cell receptor (CTLA-4、OX-40、CD137)

Treatment and study plan

golidocitinib

Drug

Daily dosing of golidocitinib

Sintilimab

Drug

Sintilimab, 200mg, intravenous, every 3 weeks.

Platinum Doublet Chemotherapy

Drug

Pemetrexed or nab-paclitaxel +carboplatin, intravenous, every 3 weeks for 2 cycles

Primary outcomes

  1. Overall response rate (ORR) (cohort1)

    Time frame: through study completion, an average of 1 year

    Complete response (CR) or partial response (PR) per investigator assessment according to RECIST 1.1

  2. Progression-free survival (PFS) (cohort2)

    Time frame: through study completion, an average of 1 year

    Time from first administration of study drug to first documented disease progression or death per investigator assessment according to RECIST 1.1

Secondary outcomes

  1. Overall survival (OS)

    Time frame: through study completion, up to 36 months

    time from first administration of study drug to death

  2. Incidence of Adverse Events

    Time frame: through study completion, up to 36 months

    Frequency an severity of AEs according to the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.

Study contacts

Contact information is provided by the study sponsor or research team.

Jie Wang, MD,PhD

CONTACT

[email protected]

010-87788219

Sponsors and collaborators

Lead sponsor

Cancer Institute and Hospital, Chinese Academy of Medical Sciences

Other

Collaborators

  • Dizal Pharmaceuticals

Registry information

Official study title

A Phase 2, Open-label, Single Arm Study to Investigate the Safety and Efficiency of Golidocitinib in Combination With Sintilimab in Patients With Locally Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC) With PD-L1TPS ≥ 1%)

Acronym: JACKPOT33

Important dates

Study start
2024
Primary completion
2026
Study completion
2027
First posted
Jan 10, 2024
Registry last updated
Jan 10, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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